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(+)-8-bromo-N-<(S)-α-methylbenzyl>-2(R)-propionamidotetralin

Base Information
  • Chemical Name:(+)-8-bromo-N-<(S)-α-methylbenzyl>-2(R)-propionamidotetralin
  • CAS No.:136925-04-7
  • Molecular Formula:C21H24BrNO
  • Molecular Weight:386.332
  • Hs Code.:
(+)-8-bromo-N-<(S)-α-methylbenzyl>-2(R)-propionamidotetralin

Synonyms:(+)-8-bromo-N-<(S)-α-methylbenzyl>-2(R)-propionamidotetralin

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Chemical Property of (+)-8-bromo-N-<(S)-α-methylbenzyl>-2(R)-propionamidotetralin
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Technology Process of (+)-8-bromo-N-<(S)-α-methylbenzyl>-2(R)-propionamidotetralin

There total 3 articles about (+)-8-bromo-N-<(S)-α-methylbenzyl>-2(R)-propionamidotetralin which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
Multi-step reaction with 3 steps
1: 70 percent / AlCl3 / CH2Cl2 / 1.25 h / -10 °C
2: 46 percent / AcOH, 4A molecular sieves, sodium cyanoborohydride / methanol; tetrahydrofuran / 3 h / 0 °C
3: 99 percent / Et3N / CH2Cl2 / 1 h / 0 °C
With aluminium trichloride; 4 A molecular sieve; sodium cyanoborohydride; acetic acid; triethylamine; In tetrahydrofuran; methanol; dichloromethane;
DOI:10.1021/jm00067a003
Guidance literature:
Multi-step reaction with 2 steps
1: 46 percent / AcOH, 4A molecular sieves, sodium cyanoborohydride / methanol; tetrahydrofuran / 3 h / 0 °C
2: 99 percent / Et3N / CH2Cl2 / 1 h / 0 °C
With 4 A molecular sieve; sodium cyanoborohydride; acetic acid; triethylamine; In tetrahydrofuran; methanol; dichloromethane;
DOI:10.1021/jm00067a003
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